NCT Number: NCT02536573
Study of Total Hip Arthroplasty Using Radlink Surgical Positioning Software
This is a prospective, randomized study of total hip arthroplasty with and without the use of Radlink surgical positioning software. The investigators are interested in discovering whether the use of the Radlink software will provide more accurate acetabular cup position when compared with surgeon estimates based on visual inspection of fluoroscopic images.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Total hip arthroplasty
Exclusion criteria
-
Treatment and study plan
Primary outcomes
-
Radiographic cup abduction angle
Time frame: 4 month postoperative
Angle of acetabular component in coronal plane measured on x-ray
-
Radiographic cup anteversion angle
Time frame: 4 month postoperative
Angle of acetabular component in sagittal plane measured on x-ray
Secondary outcomes
-
Variance of cup angles measured on x-ray
Time frame: 4 month postoperative
Statistical homogeneity of angles and how spread out the data is.
Sponsors and collaborators
Lead sponsor
Anderson Orthopaedic Research Institute
Other
Registry information
Official study title
Prospective, Randomized Study to Evaluate Total Hip Arthroplasty With and Without Radlink Surgical Positioning Software
Important dates
- Study start
- 2015
- Primary completion
- 2017
- Study completion
- 2019
- First posted
- Sep 1, 2015
- Registry last updated
- Aug 1, 2019
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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